Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance.
- NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_assertion description "[In contrast to previous reports, homozygosity for the Asp298 variant of the 894G>T polymorphism in the eNOS gene was not found to be associated with risk of AMI, extent of CAD and in-hospital mortality after AMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance.
- NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_assertion evidence source_evidence_literature NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance.
- NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_assertion SIO_000772 18495009 NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance.
- NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_assertion wasDerivedFrom gad-20150221 NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance.
- NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_assertion wasGeneratedBy ECO_0000203 NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123329.RAt5BqX68EwQpO2J6YQydTNZosCAqIRIH1zyxOW8sLLus130_provenance.